Conformationally restricted HIV-1 protease inhibitors

ABSTRACT

HIV protease inhibitors containing hydroxypyrrolidine or hydroxypiperidine with one or more basic amines are disclosed.

The present invention is concerned with compounds which inhibit the protease encoded by human immunodeficiency virus (HIV). The compounds, or pharmaceutically acceptable salts thereof, are of value in the prevention of infection by HIV, the treatment of infection by HIV and the treatment of the resulting acquired immune deficiency syndrome (AIDS).

The present invention also relates to pharmaceutical compositions containing the compounds and to a method of use of the present compounds and other agents for the treatment of AIDS & viral infection by HIV.

BACKGROUND OF THE INVENTION

A retrovirus designated human immunodeficiency virus (HIV) is the etiological agent of tile complex disease that includes progressive destruction of the immune system (acquired immune deficiency syndrome; AIDS) and degeneration of the central and peripheral nervous system. This virus was previously known as LAV, HTLV-III, or ARV. A common feature of retrovirus replication is the extensive post-translational processing of precursor polyproteins by a virally encoded protease to generate mature viral proteins required for virus assembly and function. Inhibition of this processing prevents the production of normally infectious virus. For example, Kohl, N. E., et. al., Proc. Natl. Acad, Sci. USA, 85, 4686 (1988), demonstrated that genetic inactivation of the HIV encoded protease resulted in the production of immature, non-infectious virus particles. These results indicate that inhibition of the HIV protease represents a viable method for the treatment of AIDS and the prevention or treatment of infection by HIV.

Nucleotide sequencing of HIV shows the presence of a pol gene in one open reading frame Ratner, L. et al., Nature, 313, 277(1985)!. Amino acid sequence homology provides evidence that the pol sequence encodes reverse transcriptase, an endonuclease and an HIV protease Toh, H. et al., EMBO J. 4, 1267 (1985); Power, M. D. et al., Science, 231, 1567 (1986); Pearl, L. H. et al., Nature 329, 351 (1987)!. Applicants demonstrate that the compounds of this invention are inhibitors of HIV protease.

The compounds of the present invention contain hydroxypyrrolidine or hydroxypiperidine with one or more basic amines. The particular advantages of these compounds are increased potency due to the restricted bioactive conformation.

BRIEF DESCRIPTION OF THE INVENTION

Compounds of Formula I, as herein defined, are disclosed. These compounds are useful in the inhibition of HIV protease, the prevention of infection by HIV, the treatment of infection by HIV and in the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, hydrates or esters, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS, methods of preventing infection by HIV, and methods of treating infection by HIV are also disclosed.

    ______________________________________     Designation     ______________________________________                    Protecting Group     BOC (Boc)      t-butyloxycarbonyl     CBZ (Cbz)      benzyloxycarbonyl(carbobenzoxy)     TBS (TBDMS)    t-butyl-dimethylsilyl                    Activating Group     HBT(HOBT or HOBt)                    1-hydroxybenzotriazole hydrate                    Coupling Reagent     BOP reagent    benzotriazol-l-yloxytris-                    (dimethylamino)phosphonium                    hexafluorophosphate     BOP-Cl         bis(2-oxo-3-oxazolidinyl)phosphinic                    chloride     EDC            1-ethyl-3-(3-dimethylaminopropyl)                    carbodiimide hydrochloride                    Other     (BOC).sub.2 O (BOC.sub.2 O)                    di-t-butyl dicarbonate     n-Bu.sub.4 N+F-                    tetrabutyl ammonium fluoride     nBuLi (n-Buli) n-butyllithium     DMF            dimethylformamide     Et.sub.3 N     triethylamine     EtOAc          ethyl acetate     TFA            trifluoroacetic acid     DMAP           dimethylaminopyridine     DME            dimethoxyethane     LDA            lithium diisopropylamide     THF            tetrahydrofuran                    Amino Acid     Ile            L-isoleucine     Val            L-valine     ______________________________________

DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS

This invention is concerned with the compounds of Formula I, combinations thereof, or pharmaceutically acceptable salts thereof, in the inhibition of HIV protease, the prevention of infection by HIV, the treatment of infection by HIV and in the treatment of the resulting acquired immune deficiency syndrome (AIDS). Compounds of Formula I are defined as follows: ##STR1## wherein: m=0,1;

n=0,1;

R₁ and R₂ are independently

a) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo;

b) C₅ -C₇ cycloalkyl; or

c) heterocycle unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo;

R₃ is

a) hydrogen;

b) C₁₋₆ alkyl, unsubstituted or substituted with one or more of hydroxy, C₁₋₃ alkoxy, aryl, heterocycle or halo;

c) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo;

d) heterocycle unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; or

e) a 5 to 7 membered carbocyclic or 7-10 membered bicyclic carbocyclic ring, such as cyclopentane, cyclohexane, indan, norbornane, naphthalene, thiopyran, isothiopyran, or benzopyran, the carbocyclic ring being unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; and

T is R₄ OC(O), R₄ C(O) or R₄ NR₅ C(O) wherein R₄ is

a) C₁₋₅ alkyl unsubstituted or substituted with one or more of aryl, heterocycle, hydroxy, halo or C₁₋₃ alkoxy;

b) 5-to 7-membered carbocycle or carbocycle-C₁₋₄ alkyl wherein the carbocycle is either saturated, partially saturated or unsaturated, any of which carbocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, C₁₋₃ alkoxy, halo-C₁₋₃ alkyl, aryl-C₁₋₃ alkyl, or C₃₋₅ cycloalkyl;

c) 5- to 7-membered heterocycle or heterocyclic-C₁₋₄ alkyl wherein the heterocycle has one or two heteroatoms selected from O, N or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo, C₃₋₅ cycloalkyl, or C₁₋₃ alkoxy;

d) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; or

e) heterocycle; and

R₅ is

a) hydrogen, or

b) C₁₋₄ alkyl unsubstituted or substituted with one or more of C₂₋₄ alkenyl, C₁₋₃ alkoxy, halo-C₁₋₃ alkyl, hydroxy-C₂₋₄ alkyl, aryl-C₁₋₃ alkyl, or C₃₋₅ cycloalkyl; and

A is absent or

a) an L-amino acid chosen from valine, isoleucine, leucine, alanine, asparagine or serine; or

b) a 5- to 7-membered heterocycle or heterocycle-C₁₋₄ alkyl wherein heterocycle has one or two heteroatoms selected from O, N or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo, C₃₋₅ cycloalkyl, or C₁₋₃ alkoxy,

or pharmaceutically acceptable salt thereof.

The compounds of the present invention may have asymmetric centers and occur as racemates, racemic mixtures and as individual diastereomers or enantiomers, or mixtures thereof, with all isomeric forms being included in the present invention.

When any variable (e.g., heterocycle, R₁ or R₂, etc.) occurs more than one time in any constituent or in Formula I, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

As used herein except where noted, "alkyl" is intended to include both branched- and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms (Me is methyl, Et is ethyl, Pr is propyl, Bu is butyl); "alkoxy" represents an alkyl group of indicated number of carbon atoms attached through an oxygen bridge. "Alkenyl" is intended to include a hydrocarbon chain of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, butenyl, pentenyl, and the like. "Halo", as used herein, means fluoro, chloro, bromo or iodo.

As used herein, with exceptions as noted, "aryl" is intended to mean phenyl (Ph) or naphthyl. "Carbocyclic" is intended to mean any stable 5- to 7-membered carbon ring or 7- to 10-membered bicyclic carbon ring, any of which may be saturated or partially unsaturated.

The term heterocycle or heterocyclic, as used herein except where noted, represents a stable 5- to 7-membered mono- or bicyclic or stable 7- to 10-membered bicyclic heterocyclic ting system, any ring of which may be saturated or unsaturated, and which consists of carbon atoms and from one to three heteroatoms selected from the group consisting of N, O and S, and wherein the nitrogen and sulfur heteroatoms may optionally be oxidized, and including any bicyclic group in which any of the above-defined heterocyclic tings is fused to a benzene ring. The heterocyclic ring may be attached at any heteroatom or carbon atom which results in the creation of a stable structure. Examples of such heterocyclic elements include piperidinyl, piperazinyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, 2-oxoazepinyl, azepinyl, pyrrolyl, 4-piperidonyl, pyrrolidinyl, pyrazolyl, pyrazolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, quinuclidinyl, isothiazolidinyl, indolyl, quinolinyl, isoquinolinyl, benzimidazolyl, thiadiazoyl, benzopyranyl, benzothiopyranyl, tetrahydrofuryl, tetrahydropyranyl, and tetrahydrothienyl, thienyl, benzothienyl, thiamorpholinyl, thiamorpholinyl sulfoxide, thiamorpholinyl sulfone and isobenzothiopyranyl.

The pharmaceutically-acceptable salts of the compounds of Formula I (in the form of water- or oil-soluble or dispersible products) include the conventional non-toxic salts or the quaternary ammonium salts of these compounds, which are formed, e.g., from inorganic or organic acids. Examples of such acid addition salts include acetate, adipate, alginate, aspanate, benzoate, bisulfate, citrate, digluconate, dodecylsulfate, fumarate, glycerophosphate, hemisulfate, hydrochloride, 2-hydroxy-ethanesulfonate, factate, maleate, methanesulfonate, succinate and tartrate.

In a preferred embodiment of this invention,

A is absent;

T is R₄ OC(O);

R₁ and R₂ are independently phenyl or cyclohexyl, any of which is unsubstituted or substituted with hydroxy or C₁₋₃ alkoxy;

R₃ is C₁₋₅ alkyl, unsubstituted or substituted with one or more of hydroxy or R₃ is l(S)(2(R)-hydroxyindan);

R₄ is a C₁₋₅ alkyl or a 5- to 7-membered heterocycle having one heteroatom selected from O or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo or C₁₋₃ alkoxy.

A second embodiment is further limited to compounds wherein:

T is R₄ OC(O);

R₁ and R₂ are phenyl;

R₃ is t-butyl, 2-methylpropyl or 1(S)(2(R)-hydroxyindan); and

R₄ is

i) C₁₋₅ alkyl; or

ii) 1,1-dioxo-tetrahydrothienyl or tetrahydrofuranyl, unsubstituted or substituted with C₁₋₄ alkyl, C₂₋₄ alkenyl or C₁₋₃ alkoxy.

A third embodiment is further limited to compound wherein:

R₄ is

i) C₁₋₅ alkyl; or

ii) tetrahydrofuran-3-yl or 1,1-dioxotetrahydrothien-3-yl, unsubstituted or substituted with methyl, ethyl, n-propyl, i-propyl, methoxy, ethoxy, or propenyl.

In a fourth preferred embodiment,

R₁ and R₂ are phenyl;

R₃ is 1(S)(2(R)-hydroxyindan); and

R₄ is a C₁₋₅ alkyl or 5- to 7-membered heterocycle having one S heteratom, said heterocycle unsubstituted or substituted with one or more of C₁₋₄ alkyl, oxo or C₃₋₅ cycloalkyl.

A fifth embodiment is further limited to:

R₁ and R₂ are phenyl;

R₃ is l(S)(2(R)-hydroxyindan);

R₄ is

i) C₁₋₅ alkyl; or

ii) 1,1-dioxotetrahydrothien-3-yl, unsubstituted or substituted with C₁₋₄ alkyl, or C₃₋₅ cycloalkyl.

Most preferred compounds of this invention include the following:

Compound A ##STR2## N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(S)-hydroxy-3'(S)-(1"(S)-ten-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane-amide; or Compound B ##STR3## N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(R)-hydroxy-3'(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane-amide; or Compound C ##STR4## N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(4'(S)-hydroxy-4'(S)-(1"(S)-ten-butyloxycarbonylamino-2"-phenylethyl)piperidinyl)-3-phenylpropane-amide; or Compound D ##STR5## N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(4'-hydroxy-4'-(1"(S)-(3"'(S)-tetrahydrofuryloxycarbonyl)amino-2"-phenyl)ethyl-1'-piperidinyl)-3-phenylpropane-amide; or Compound E ##STR6## N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(3'(S)-hydroxy-3'(S)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)-1'-piperidinyl)-3-phenylpropane-amide; or Compound F ##STR7## named, N-(1',1'-dimethylethyl)-2(S)-(3'(R)-hydroxy-3'(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)-1'-piperidinyl)-3-cyclohexylpropaneamide; or pharmaceutically acceptable salt thereof.

The compounds of the present invention are prepared in accordance with Schemes I-IV. ##STR8## Compound 2 is prepared by coupling of compound 1 with methoxymethylamine under the effect of N-methylpiperidine and methyl chloroformate. Reaction of Compound 2 with allylmagnesium bromide provides compound 3, which is convened to compound 4 by addition of vinylmagnesium bromide. Compound 4 is protected as oxazolidinone 5.Ozonolysis of compound 5 followed by condensation with amine 11 under reductive amination conditions provides compound 6. Hydrolysis of the protecting group in compound 6 gives compound 7. The amine 11 is prepared from the coupling of an amino acid 8 and amine 9 followed by deprotection of the tert-butyloxycarbonyl group of compound 10. Example 1 illustrates but does not limit Scheme 1. ##STR9## Compound 12 is obtained from the reaction of compound 2 with vinylmagnesium bromide. Addition of allylmagnesium bromide to compound 12 was effected under the influence of CeCl₃ to provide compound 13. Compound 16 is then prepared from compound 13 in the same manner as compound 6 was prepared from compound 4. Example 2 illustrates but does not limit Scheme 2. ##STR10## Compound 17 was prepared from compound 2 using 3-butenylmagnesium bromide. Addition of vinylmagnesium bromide to compound 17 provides compound 18. Reaction of compound 3 with allylmagnesium bromide provides compound 20. Reaction of compound 2 with 2-methyl-1-propenylmagnesim bromide provides compound 22 which was convened to compound 23 by addition of 3-butenylmagnesium bromide. From compounds 18, 20, and 23 compounds 19, 21, and 24 are prepared, respectively, according to the same method that was used for the preparation of compound 6 from 5. Examples 3-5 illustrate but does not limit Scheme 3. ##STR11## Treatment of compound 7, 16, 19, 21 or 24 with gaseous HCl in cold EtOAC or trifluoroacetic acid in dichloromethane provides the amine 25. Coupling of compound 25 with N-protected amino acid under the effect of HBT, EDC in DMF yields compound 26. Compound 28 is prepared by the reaction of compound 25 with compound 27 in the presence of triethylamine in dichloromethane or acetonitrile.

Other substituents for X, R₁, R₂, R₃ and R₄ in Formula I are readily prepared by those skilled in the art, by substituting and/or protecting appropriate groups in the schemes outlined above.

The compounds of the present invention include but are not limited to those of the following Table 1:

                                      TABLE I     __________________________________________________________________________      ##STR12##     R.sub.1           R.sub.2                 R.sub.3      T     __________________________________________________________________________     Ph    Ph                  ##STR13##                               ##STR14##     Ph    Ph                  ##STR15##                               ##STR16##     Ph    Ph                  ##STR17##                               ##STR18##     Ph    Ph                  ##STR19##                               ##STR20##     Ph            ##STR21##                  ##STR22##                               ##STR23##      ##STR24##           Ph                  ##STR25##                               ##STR26##      ##STR27##           Ph                  ##STR28##                               ##STR29##      ##STR30##           Ph                  ##STR31##                               ##STR32##     Ph    Ph                  ##STR33##                               ##STR34##     Ph    Ph                  ##STR35##                               ##STR36##     Ph    Ph                  ##STR37##                               ##STR38##     Ph    Ph                  ##STR39##                               ##STR40##     Ph            ##STR41##                  ##STR42##                               ##STR43##      ##STR44##           Ph                  ##STR45##                               ##STR46##      ##STR47##           Ph                  ##STR48##                               ##STR49##      ##STR50##           Ph                  ##STR51##                               ##STR52##     Ph    Ph                  ##STR53##                               ##STR54##     Ph    Ph                  ##STR55##                               ##STR56##     Ph    Ph                  ##STR57##                               ##STR58##     Ph    Ph                  ##STR59##                               ##STR60##     Ph            ##STR61##                  ##STR62##                               ##STR63##      ##STR64##           Ph                  ##STR65##                               ##STR66##      ##STR67##           Ph                  ##STR68##                               ##STR69##     Ph    Ph                  ##STR70##                               ##STR71##     Ph    Ph                  ##STR72##                               ##STR73##     Ph    Ph                  ##STR74##                               ##STR75##     Ph    Ph                  ##STR76##                               ##STR77##     Ph            ##STR78##                  ##STR79##                               ##STR80##      ##STR81##           Ph                  ##STR82##                               ##STR83##      ##STR84##           Ph                  ##STR85##                               ##STR86##      ##STR87##           Ph                  ##STR88##                               ##STR89##     __________________________________________________________________________

                                      TABLE II     __________________________________________________________________________      ##STR90##     R.sub.1           R.sub.2                 R.sub.3      T     __________________________________________________________________________     Ph    Ph                  ##STR91##                               ##STR92##     Ph    Ph                  ##STR93##                               ##STR94##     Ph    Ph                  ##STR95##                               ##STR96##     Ph    Ph                  ##STR97##                               ##STR98##     Ph            ##STR99##                  ##STR100##                               ##STR101##      ##STR102##           Ph                  ##STR103##                               ##STR104##      ##STR105##           Ph                  ##STR106##                               ##STR107##      ##STR108##           Ph                  ##STR109##                               ##STR110##     Ph    Ph                  ##STR111##                               ##STR112##     Ph    Ph                  ##STR113##                               ##STR114##     Ph    Ph                  ##STR115##                               ##STR116##     Ph    Ph                  ##STR117##                               ##STR118##     Ph            ##STR119##                  ##STR120##                               ##STR121##      ##STR122##           Ph                  ##STR123##                               ##STR124##      ##STR125##           Ph                  ##STR126##                               ##STR127##      ##STR128##           Ph                  ##STR129##                               ##STR130##     Ph    Ph                  ##STR131##                               ##STR132##     Ph    Ph                  ##STR133##                               ##STR134##     Ph    Ph                  ##STR135##                               ##STR136##     Ph    Ph                  ##STR137##                               ##STR138##     Ph            ##STR139##                  ##STR140##                               ##STR141##      ##STR142##           Ph                  ##STR143##                               ##STR144##      ##STR145##           Ph                  ##STR146##                               ##STR147##      ##STR148##           Ph                  ##STR149##                               ##STR150##     Ph    Ph                  ##STR151##                               ##STR152##     Ph    Ph                  ##STR153##                               ##STR154##     Ph    Ph                  ##STR155##                               ##STR156##     Ph    Ph                  ##STR157##                               ##STR158##     Ph            ##STR159##                  ##STR160##                               ##STR161##      ##STR162##           Ph                  ##STR163##                               ##STR164##      ##STR165##           Ph                  ##STR166##                               ##STR167##      ##STR168##           Ph                  ##STR169##                               ##STR170##     __________________________________________________________________________

The compounds of the present invention are useful in the inhibition of HIV protease, the prevention or treatment of infection by the human immunodeficiency virus (HIV) and the treatment of consequent pathological conditions such as AIDS. Treating AIDS or preventing or treating infection by HIV is defined as including, but not limited to, treating a wide range of states of HIV infection: AIDS, ARC (AIDS related complex), both symptomatic and asymtomatic, and actual or potential exposure to HIV. For example, the compounds of this invention are useful in treating infection by HIV after suspected past exposure to HIV by e.g., blood transfusion, accidental needle stick, or exposure to patient blood during surgery.

The compounds of this invention are also useful in the preparation and execution of screening assays for antiviral compounds. For example, the compounds of this invention are useful for isolating enzyme mutants, which are excellent screening tools for more powerful antiviral compounds. Furthermore, the compounds of this invention are useful in establishing or determining the binding site of other antivirals to HIV protease, e.g., by competitive inhibition. Thus the compounds of this invention are commercial products to be sold for these purposes.

For these purposes, the compounds of the present invention may be administered orally, parenterally (including subcutaneous injections, intravenous, intramuscular, intrastemal injection or infusion techniques), by inhalation spray, or rectally, in dosage unit formulations containing conventional non-toxic pharmaceutically-acceptable carriers, adjuvants and vehicles.

Thus, in accordance with the present invention there is further provided a method of treating and a pharmaceutical composition for treating HIV infection and AIDS. The treatment involves administering to a patient in need of such treatment a pharmaceutical composition comprising a pharmaceutical carrier and a therapeutically-effective amount of a compound of the present invention, or a pharmaceutically-acceptable salt thereof.

These pharmaceutical compositions may be in the form of orally-administrable suspensions or tablets; nasal sprays; sterile injectable preparations, for example, as sterile injectable aqueous or oleagenous suspensions or suppositories.

When administered orally as a suspension, these compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may contain microcrystalline cellulose for imparting bulk, alginic acid or sodium alginate as a suspending agent, methylcellulose as a viscosity enhancer, and sweetners/flavoring agents known in the art. As immediate release tablets, these compositions may contain microcrystalline cellulose, dicalcium phosphate, starch, magnesium stearate and lactose and/or other excipients, binders, extenders, disintegrants, diluents and lubricants known in the art.

When administered by nasal aerosol or inhalation, these compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, flourocarbons, and/or other solubilizing or dispersing agents known in the art.

The injectable solutions or suspensions may be formulated according to known art, using suitable non-toxic, parenterally-acceptable diluents or solvents, such as mannitol, 1,3-butanediol, water, Ringer's solution or isotonic sodium chloride solution, or suitable dispersing or wetting and suspending agents, such as sterile, bland, fixed oils, including synthetic mono- or diglycerides, and fatty acids, including oleic acid.

When rectally administered in the form of suppositories, these compositions may be prepared by mixing the drug with a suitable non-irritating excipient, such as cocoa butter, synthetic glyceride esters or polyethylene glycols, which are solid at ordinary temperatures, but liquidify and/or dissolve in the rectal cavity to release the drug.

Dosage levels of the order of 0.02 to 5.0 or 10.0 grams-per-day are useful in the treatment or prevention of the above-indicated conditions, with oral doses two-to-five times higher. For example, infection by HIV is effectively treated by the administration of from 1.0 to 50 milligrams of the compound per kilogram of body weight from one to three times per day. It will be understood, however, that the specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age of the patient, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy.

The present invention is also directed to combinations of the HIV protease-inhibitory compounds with one or more agents useful in the treatment of AIDS.

                  TABLE C     ______________________________________     Drug Name    Manufacturer   Indication     ______________________________________     ANTIVIRALS     AL-721       Ethigen        ARC, PGL                  (Los Angeles, CA)                                 HIV positive,                                 AIDS     Recombinant Human                  Triton Biosciences                                 AIDS, Kaposi's     Interferon Beta                  (Almeda, CA)   sarcoma, ARC     Acemannan    Carrington Labs                                 ARC                  (Irving, TX)   (See also                                 immuno-                                 modulators)     Cytovene     Syntex         sight                                 threatening CMV     Ganciclovir  (Palo Alto, CA)                                 peripheral CMV                                 retinitis     d4T          Bristol-Myers  AIDS, ARC     Didehydrodeoxy-                  (New York, NY)     thymidine     ddI          Bristol-Myers  AIDS, ARC     Dideoxyinosine                  (New York, NY)     EL10         Elan Corp, PLC HIV infection                  (Gainesville, GA)                                 (See also                                 immuno-                                 modulators)     Trisodium    Astra Pharm.   CMV retinitis,     Phosphonoformate                  Products, Inc  HIV infection,                  (Westborough, MA)                                 other CMV                                 infections     Dideoxycytidine;                  Hoffman-La Roche                                 AIDS, ARC     ddC          (Nutley, NJ)     Novapren     Novaferon Labs, Inc.                                 HIV inhibitor                  (Akron, OH)                  Diapren, Inc.                  (Roseville, MN,                  marketer)     Peptide T    Peninsula Labs AIDS     Octapeptide  (Belmont, CA)     Sequence     Zidovudine; AZT                  Burroughs Wellcome                                 AIDS, adv, ARC     AIDS, adv, ARC                  (Rsch. Triangle Park,                                 pediatric AIDS,                  NC)            Kaposi's sarcoma,                                 asymptomatic                                 HIV infection,                                 less severe                                 HIV disease,                                 neurological                                 involvement, in                                 combination with                                 other therapies.     Ansamycin LM 427                  Adria Laboratories                                 ARC                  (Dublin, OH)                  Erbamont                  (Stamford, CT)     Dextran Sulfate                  Ueno Fine Chem.                                 AIDS, ARC,                  Ind. Ltd.      HIV positive                  (Osaka, Japan) asymptomatic     Virazole     Viratek/ICN    asymptomatic     Ribavirin    (Costa Mesa, CA)                                 HIV positive,                                 LAS, ARC     Alpha Interferon                  Burroughs Wellcome                                 Kaposi's sarcoma,                  (Rsch. Triangle                                 HIV in combina-                  Park, NC)      tion w/Retrovir     Acyclovir    Burroughs Wellcome                                 AIDS, ARC,                                 asymptomatic                                 HIV positive,                                 in combination                                 with AZT.     Antibody which                  Advanced Biotherapy                                 AIDS, ARC     neutralizes pH                  Concepts     labile alpha aberrant                  (Rockville, MD)     Interferon in an     immuno-adsorption     column     661          Merck          AIDS, ARC,                  (Rahway, NJ)   asymptomatic                                 HIV positive,                                 also in combina-                                 tion with AZT.     229          Merck          AIDS, ARC,                  (Rahway, NJ)   asymptomatic                                 HIV positive,                                 also in combina-                                 tion with AZT.     Nevirapine   Boehringer     AIDS, ARC,                  Ingelheim      asymptomatic                                 HIV positive,                                 also in combina-                                 tion with AZT.     IMMUNO-MODULATORS     AS-101       Wyeth-Ayerst Labs.                                 AIDS                  (Philadelphia, PA)     Bropirimine  Upjohn         advanced AIDS                  (Kalamazoo, MI)     Acemannan    Carrington Labs, Inc.                                 AIDS, ARC                  (Irving, TX)   (See also anti-                                 virals)     CL246,738    American Cyanamid                                 AIDS, Kaposi's                  (Pearl River, NY)                                 sarcoma                  Lederle Labs                  (Wayne, NJ)     EL10         Elan Corp, PLC HIV infection                  (Gainesville, GA)                                 (See also anti-                                 virals)     Gamma Interferon                  Genentech      ARC, in combina-                  (S. San Francisco,                                 tion w/TNF                  CA)            (tumor necrosis                                 factor)     Granulocyte  Genetics Institute                                 AIDS     Macrophage Colony                  (Cambridge, MA)     Stimulating  Sandoz     Factor       (East Hanover, NJ)     Granulocyte  Hoeschst-Roussel                                 AIDS     Macrophage Colony                  (Sommerville, NJ)     Stimulating  Immunex     Factor       (Seattle, WA)     Granulocyte  Schering-Plough                                 AIDS     Macrophage Colony                  (Madison, NJ)     Stimulating Factor          AIDS, in combi-                                 nation w/AZT     HIV Core Particle                  Rorer          seropositive     Immunostimulant                  (Ft. Washington, PA)                                 HIV     IL-2         Cetus          AIDS, in combi-     Interleukin-2                  (Emeryville, CA)                                 nation w/AZT     IL-2         Hoffman-La Roche                                 AIDS, ARC,     Interleukin-2                  (Nutley, NJ)   HIV, in combina-                  Immunex        tion w/AZT     Immune Globulin                  Cutter Biological                                 pediatric AIDS,     Intravenous  (Berkeley, CA) in combination     (human)                     w/AZT     IMREG-1      Imreg          AIDS, Kaposi's                  (New Orleans, LA)                                 sarcoma, ARC,                                 PGL     IMREG-2      Imreg          AIDS, Kaposi's                  (New Orleans, LA)                                 sarcoma, ARC,                                 PGL     Imuthiol Diethyl                  Merieux Institute                                 AIDS, ARC     Dithio Carbamate                  (Miami, FL)     Alpha-2      Schering Plough                                 Kaposi's sarcoma     Interferon   (Madison, NJ)  w/AZT: AIDS     Methionine-  TNI Pharmaceutical                                 AIDS, ARC     Enkephalin   (Chicago, IL)     MTP-PE       Ciba-Geigy Corp.                                 Kaposi's sarcoma     Muramyl-     (Summit, NJ)     Tripeptide     Granulocyte  Amgen          AIDS, in combi-     Colony Stimulating                  (Thousand Oaks, CA)                                 nation w/AZT     Factor     rCD4         Genentech      AIDS, ARC     Recombinant  (S. San Francisco,     Soluble Human CD4                  CA)     rCD4-IgG                    AIDS, ARC     hybrids     Recombinant  Biogen         AIDS, ARC     Soluble Human CD4                  (Cambridge, MA)     Interferon   Hoffman-La Roche                                 Kaposi's sarcoma     Alfa 2A      (Nutley, NJ)   AIDS, ARC, in                                 combination                                 w/AZT     SK&F106528   Smith, Kline & HIV infection     Soluble T4   French Laboratories                  (Philadelphia, PA)     Thymopentin  Immunobiology  HIV infection                  Research Institute                  (Annandale, NJ)     Tumor Necrosis                  Genentech      ARC, in combi-     Factor; TNF  (S. San Francisco,                                 nation w/gamma                  CA)            Interferon     ANTI-INFECTIVES     Clindamycin with                  Upjohn         PCP     Primaquine   (Kalamazoo, MI)     Fluconazole  Pfizer         cryptococcal                  (New York, NJ) meningitis,                                 candidiasis     Pastille     Squibb Corp.   prevention of     Nystatin Pastille                  (Princeton, NJ)                                 oral candidiasis     Ornidyl      Merrell Dow    PCP     Eflornithine (Cincinnati, OH)     Pentamidine  LyphoMed       PCP treatment     Isethionate (IM & IV)                  (Rosemont, IL)     Trimethoprim                antibacterial     Trimethoprim/sulfa          antibacterial     Piritrexim   Burroughs Wellcome                                 PCP treatment                  (Rsch. Triangle                  Park, NC)     Pentamidine  Fisons Corporation                                 PCP prophylaxis     isethionate for                  (Bedford, MA)     inhalation     Spiramycin   Rhone-Poulenc  cryptosporidial                  Pharmaceuticals                                 diarrhea                  (Princeton, NJ)     Intraconazole-                  Janssen Pharm. histoplasmosis;     R51211       (Piscataway, NJ)                                 cryptococcal                                 meningitis     Trimetrexate Warner-Lambert PCP     OTHER     Recombinant Human                  Ortho Pharm. Corp.                                 severe anemia     Erythropoietin                  (Raritan, NJ)  assoc. with AZT                                 therapy     Megestrol Acetate                  Bristol-Myers  treatment of                  (New York, NY) anorexia assoc.                                 w/AIDS     Total Enteral                  Norwich Eaton  diarrhea and     Nutrition    Pharmaceuticals                                 malabsorption                  (Norwich, NY)  related to AIDS     ______________________________________

It will be understood that the scope of combinations of the compounds of this invention with AIDS antivirals, immunomodulators, anti-infectives or vaccines is not limited to the list in the above Table, but includes in principle any combination with any pharmaceutical composition useful for the treatment of AIDS.

Certain compounds of Table C are the following: 661 is 3-( 4,7-dichloro-1,3-benzoxazol-2-yl )methyl!-amino)-5-ethyl-6-methyl-pyridin-2(1H)-one; 229 is 3- 2-(1,3-benzoxazol-2-yl)-ethyl!-5-ethyl-6-methyl-pyridin-2(1H)-one. The synthesis of 661 and 229 is described in EPO 48407 1, and EPO 462800, both herein incorporated by reference. The synthesis of ddC, ddI and AZT are also described in EPO 484071.

Preferred combinations are simultaneous or alternating treatments of an inhibitor of HIV protease and a non-nucleoside inhibitor of HIV reverse transcriptase. An optional third component in the combination is a nucleoside inhibitor of HIV reverse transcriptase, such as AZT, ddC or ddI. A preferred inhibitor of HIV protease is Compound A. Preferred non-nucleoside inhibitors of HIV reverse transcriptase include Compound B, Compound C or nevirapine. These combinations may have synergistic effects on limiting the spread of HIV. Preferred combinations include the following (1) Compound A, with a preferred non-nucleoside inhibitor of HIV reverse transcriptase, and, optionally, AZT or ddI or ddC; (2) Compound A, and any of AZT or ddI or ddC.

ASSAY FOR INHIBITION OF MICROBIAL EXPRESSED HIV PROTEASE

Inhibition studies of the reaction of the protease expressed in Eschericia coli with a peptide substrate Val-Ser-Gln-Asn-(betanapthyl)Ala-Pro-Ile-Val, 0.5 mg/mL at the time the reaction is initiated! were in 50 mM Na acetate, pH 5.5, at 30° C. for 1 hour. Various concentrations of inhibitor in 1.0 ml DMSO were added to 25 ml of the peptide solution in water. The reaction is initiated by the addition of 15 ml of 0.33 nM protease (0.11 ng) in a solution of 0.133 M Na acetate pH 5.5 and 0.1% bovine serum albumin. The reaction was quenched with 160 ml of 5% phosphoric acid. Products of the reaction were separated by HPLC (VYDAC wide pore 5 cm C-18 reverse phase, acetonitrile gradient, 0.1% phosphoric acid). The extent of inhibition of the reaction was determined from the peak heights of the products. HPLC of the products, independently synthesized, proved quantitation standards and confirmation of the product composition. Compounds A-H showed IC₅₀ values ranging 200→3,000 nM.

CELL SPREAD ASSAY

Inhibition of the spread of HIV in cell culture was measured according to Nunberg, J. H. et al., J. Virol. 65, 4887 (1991). In this assay, MT-4 T-lymphoid cells were infected with HIV-1 (wild-type, unless otherwise indicated) by using a predetermined inoculum, and cultures were incubated for 24 h. At this time, ≦1% of the cells were positive by indirect immunofluorescence. Cells were then extensively washed and distributed into 96-well culture dishes. Serial twofold dilutions of inhibitor were added to the wells, and cultures were continued for 3 additional days. At 4 days postinfection, 100% of the cells in control cultures were infected. HIV-1 p24 accumulation was directly correlated with virus spread. The cell culture inhibitory concentration was defined as the inhibitor concentration in nanomoles/liter which reduced the spread of infection by at least 95%, or CIC₉₅.

INHIBITION OF VIRUS SPREAD A. Preparation of HIV-infected MT-4 cell Suspension

MT cells were infected at Day 0 at a concentration of 250,000 per ml with a 1:1000 dilution of HIV-1 strain IIlb stock (final 125 pg p24/ml; sufficient to yield ≦1% infected cells on day 1 and 25-100% on day 4). Cells were infected and grown in the following medium: RPMI 1640 (Whittaker BioProducts), 10% inactivated fetal bovine serum, 4 mM glutamine (Gibco Labs) and 1:100 Penicillin-Streptomycin (Gibco Labs).

The mixture was incubated overnight at 37° C. in 5% CO₂ atmosphere.

B. Treatment with Inhibitors

A matrix of nanomolar range concentrations of the pairwise combinations is prepared. At Day 1, aliquots of 125 ml of inhibitors are added to equal volumes of HIV-infected MT-4 cells (50,000 per well) in a 96-well microtiter cell culture plate. Incubation is continued for 3 days at 37° C. in 5% CO₂ atmosphere.

C. Measurement of Virus Spread

Using a multichannel pipettor, the settled cells are resuspended and 125 ml harvested into a separate microtiter plate. The supernatant is assayed for HIV p24 antigen.

The concentration of HIV p24 antigen is measured by an enzyme immunoassay, described as follows. Aliquots of p24 antigen to be measured are added to microwells coated with a monoclonal antibody specific for HIV core antigen. The microwells are washed at this point, and at other appropriate steps that follow. Biotinylated HIV-specific antibody is then added, followed by conjugated streptavidin-horseradish peroxidase. A color reaction occurs from the added hydrogen peroxide and the concentration of HIV p24 antigen.

Calculation of Degree of Synergy

When there is synergy pairwise combinations of inhibitors are found to exhibit markedly enhanced inhibition of virus spread, in comparison to each inhibitor alone, or in comparison to merely additive inhibition of each inhibitor.

The data is processed as follows: fractional inhibitory concentration ratios (FIC) are calculated according to Elion, et al., J. Biol. Chem., 208, 477 (1954). The minimum sum of FICS, which is the maximum synergy, is determined for. various pairwise combinations. The smaller the number, the greater the synergy.

EXAMPLE 1 Step 1 Preparation of N',N'-methoxymethyl-N-tert-butyloxycarbonylphenylalanine-carboxamide, compound 2

N,O-dimethylhydroxylamine hydrochloride (3.102 g, 31.8 mmol) in 20 mL dichloromethane was placed in a 100 mL 3-neck flask equipped with a magnetic stirrer, digital thermometer, nitrogen inlet tube and a dropping funnel. The suspension was stirred at 0° C. and N-methylpiperidine (3.92 mL, 32.3 mmol) was added dropwise to maintain the internal temperature at 2°±2° C. A clear colorless solution resulted. In a 1 L 3-neck flask equipped with a magnetic stirrer, nitrogen inlet tube, dropping funnel and digital thermometer was placed 7.96 g (30.0 mmol) of L-phenylalanine in 35 mL of dry THF and 120 mL of dry dichloromethane. The solution was stirred at -20° C. and N-methylpiperidine (3.92 mL, 32.3 mmol) was added rapidly via dropping funnel. Temperature rose to 5° C. Methylchloroformate (2.48 mL, 32.1 mmol) was added rapidly keeping the reaction temperature at -15° C. After 5 min, previously prepared N,O-dimethylhydroxylamine solution was added keeping the reaction temperature at -12°±1° C. After completing the addition, the cooling bath was removed and the clear reaction mixture was warmed to room temperature and stirring was continued overnight (15 h). The reaction mixture was cooled to 0° C., washed with 2×40 mL 10% citric acid solution. The organic phase was cooled to 0° C. and washed with 2×40 mL of NaOH solution and 40 mL of brine. It was dried over anhyd MgSO₄ and filtered and concentrated under reduced pressure (bath temperature<30° C.). When the residue was dried under high vacuum, 8.791 g of colorless oil was obtained (95% yield). ¹ H NMR (CDCl₃) 1.39 (9H, s), 2.88 (1H, ABX, J_(AB) =13.0 Hz, J_(AX) =7.6 Hz), 3.05 (1H, J_(AB) =13.2 Hz, J_(BX) =6.4 Hz), 3.17 (3H, s), 3.66 (3H, s), 4.96 (1H, m), 5.28 (1H, d, 7.6 Hz), 7.24-7.42 (5H, m).

Step 2 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-1-phenyl-5-hexen-3-one compound 3

To a magnetically stirred solution of allylmagnesium bromide in ether (1.0 M solution, 12.97 mL, 12.97 mmol) was added 15 mL of dry THF. The mixture was cooled to -78° C. and N',N'methoxymethyl-N-tert-butyloxycarbonylphenylalanine-carboxamide in THF (10 mL) was added dropwise over a period of 10 min. Stirring was continued for ˜1 h and the flask was allowed to warm up to room temperature. When there was no starting material by TLC, 10% citric acid solution (20 mL) was added to the mixture and it was extracted with ethyl ether (20 mL×3) and the ether extracts were combined. The combined organic solution was washed with sat aq NaHCO₃ solution (20 mL), water (20 mL), and brine (20 mL), and dried over anhyd MgSO₄. Filtered solution was concentrated to give 1.49 g (99% yield) of a colorless residue. ¹ H NMR (CDCl₃) 7.15-7.35 (5H, m), 5.83-5.92 (1 H, m), 5.05-5.21 (3H, m), 4.59 (1H, m), 2.95-3.26 (4H, m), 1.41 (9H, s).

Step 3 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-ethenyl-3(S)-hydroxy-1-phenyl-5-hexene, compound 4

To a magnetically stirred solution of vinylmagnesium bromide in ether (1.0 M, 10.4 mL) at -40° C. was added a THF solution (5 mL) of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-1-phenyl-5-hexen-3-one (0.752 g, 2.60 mmol) over a period of 5 min. The mixture was stirred for 1 h at -40≠-30° C. and then slowly warmed up to room temperature over a period of 2 h. After addition of 10% aq citric acid solution (10 mL), the mixture was diluted with ether (10 mL) and layers separated. The aq layer was extracted with ether (2×5 mL) the organic layers combined. Combined organic layers were washed with sat aq NaHCO₃ solution (10 mL) and brine (15 mL). Drying (over anhyd MgSO₄) followed by concentration provided a crude product, which was purified on a silica gel chromatographic column to provide 0.396 g (50%) of desired product. ¹ H NMR (CDCl₃) 7.15-7.32 (5H, m), 5.95 (1H, dd, J=12, 17 Hz), 5.84 (1H, m), 5.37 (1H, d, J=18 Hz), 5.16-5.28 (3H, m), 4.46 (1H, d, J=7.6 Hz), 3.82 (1H, m), 3.18 (1H, ABX, J_(AB) =14.0, J_(AX) =5.1 Hz), 2.69 (1H, ABX, J_(AB) =14.1, J_(BX) =12Hz), 2.48 (2H, d, J=7.0 Hz), 1.95 (1H, br s), 1.27 (9H, s).

Step 4 Preparation of (4S)-phenylmethyl-3-N-(1,1-dimethylethoxy-carbonyl)-5(S)-ethenyl-5(S)-(2'-propenyl)oxazolidin-2-one, compound 5

To a magnetically stirred solution of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-ethenyl-3(S)-hydroxy-1-phenyl-5-hexene (0.833 g, 2.00 mmol) in 10 mL THF was added NaH (60% dispersion in mineral oil, 0.314 g, 7.86 mmol) and stirring was continued for 0.5 h. Carbonyldiimidazole (0.637 g, 3.93 mmol) and Boc-anhydride (1.144 g, 5.24 mmol) were added and the mixture was stirred for 4 h. Sat aq NH₄ Cl solution (10 mL) was added to the reaction mixture and it was extracted with EtOAC (15 mL×3). The combined organic layers were dried over anhyd Na₂ SO₄, filtered and concentrated under reduced pressure. Silica gel column chromatography (10% EtOAc in hexane) furnished a white solid (0.738 g, 82% yield). mp 104°-105.5° C.; ¹ H NMR (CDCl₃) 7.25-7.38 (5H, m), 5.70 (1H, dd, I=10.9, 17.2 Hz), 5.66 (1H, m), 5.12-5.40 (3H, m), 5.11 (1H, dd, J=1.2, 16.9 Hz), 4.40 (1H, dr, J=6.9, 7.2 Hz), 3.08 (1H, dd, J=3.0, 6.7 Hz), 2.73 (1H, ABX, J_(AB) =14.5 Hz, J_(AX) =6.5 Hz), 2.32 (1H, ABX, J_(AB) =14.5 Hz, J_(BX) =7.7 Hz), 1.38 (9H, s).

Step 5 Preparation of N-(1'(S)-(2'(R)-hydroxyindanyl)-2(S)-amino-3-phenylpropanamide compound 11

To a magnetically stirred solution of N-tert-butyloxycarbonylphenylalanine (2.653 g, 10.0 mmol) in DMF (25 mL) were added 1(S)-amino-2(R)-hydroxyindan (1.79 g, 12.0 mmol), HBT (1.486 g, 11.0 mmol) and EDC (2.109 g, 11.0 mmol). Triethylamine was added to adjust the pH of the mixture to -8.5. Stirring was continued for 15 h. DMF was removed in vacuo and the residue was partitioned between 10% aq citric acid solution (20 mL) and EtOAC (20 mL). The organic layer was washed with 10% aq citric acid solution (20 mL), sat aq NaHCO₃ solution (20 mL), and brine (20 mL) and dried over anhyd MgSO₄. The solution was filtered and concentrated to give a white solid. The crude product was recrystalized in 75% EtOAc in hexane to furnish 3.64 g (92% yield) of N-(1(S)-(2(R)-hydroxyindanyl)-2(S)-(tert-butyloxycarbonyl)amino-3-phenylpropanamide (compound 10) as a white flake. mp 147.5-148.5° C.; ¹ H NMR (CDCl₃) 7.20-7.40 (9H, m), 6.22 (1H, d, J=7.6 Hz), 5.36 (1H, rid, J=5.7, 7.6 Hz), 5.22 (1H, m), 4.44 (1H, m), 4.38 (1H, m), 3.22 (1H, dd, J=7.0, 12.7 Hz), 3.10 (1H, m), 3.07 (1H, m), 2.86 (1H, dd, J=12.7, 1.6 Hz), 1.41 (9H, s).

To a magnetically stirred solution of compound 10 (1.503 g, 3.79 mmol) in EtOAc (250 mL) at 0° C. was bubbled in dry HCl gas for 30 min. Stirring was continued for 0.5 h at 0° C. Solvent was removed under reduced pressure and the residue dissolved in dichloromethane (50 mL). The solution was washed with sat aq NaHCO₃ solution (30 mL) and brine (30 mL), dried over anhyd Na₂ SO₄, filtered and concentrated under reduced pressure. The crude product was recrystallized from MeOH/EtOAc/hexene to provide 0.947 g (84% yield) of a colorless needle. mp 180°-181° C.; ¹ H NMR (CDCl₃) 7.66 (1H, d, J=7.8 Hz), 7.15-7.38 (9H, m), 5.27 (1H, dd, J=4.9, 7.6 Hz), 4.52 (1H, br s), 3.84 (1H, dd, J=6.6, 7.0 Hz), 3.23 (1H, dd, J=5.9, 13.7 Hz), 3.11 (1 H, dd, J=4.8, 16.0 Hz), 3.03 (1 H, dd, J=8.3, 13.8 Hz), 2.90 (1H, d, J:16.7 Hz).

Step 6 Preparation of N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(S)-hydroxy-3'-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane-amide, compound 7

(4S)-Phenylmethyl-3-N-(1,1-dimethylethoxy-carbonyl)-5(S)-ethenyl-5(S)-(2'-propenyl)oxazolidin-2-one (0.060 g, 0.175 mmol) in 4 mL, methanol was cooled to -78° C. and ozone was bubbled into the solution until it turned to blue. Dimethyl sulfide (≠0.1 mL) was added at -78° C. and the mixture was allowed to warm to room temperature. Solvent was removed under reduced pressure. The residue was dissolved in methanol (3 mL) and N-(1(S)-(2(R)-hydroxyindanyl)-2(S)-amino-3-phenylpropanamide (0.062 g, 0.210 mmol) and 4Å molecular sieves were added. After stirring for 0.5 h, NaCNBH₃ (0.053 g, 0.838 mmol) and two drops of acetic acid were added. Stirring was continued for 24 h. The reaction mixture was then partitioned between sat aq Na₂ CO₃ solution (10 mL) and EtOAc (10 mL) and the aqueous layer was extracted with EtOAc (5 mL×2). Combined organic layers were so dried over anhyd Na₂ SO₄, filtered and concentrated under reduced pressure. The crude product was purified on a silica gel column chromatography (60% to 80% EtOAc in hexane) to provide 29 mg (27% yield) of compound 6 as a colorless residue.

To a magnetically stirred solution of compound 6 (0.066 g, 0.108 mmol) in 2 mL methanol was added 0.54 mL of 1 N NaOH solution. Stirring was continued for 3 h at room temperature. Solvent was removed under reduced pressure and the residue was dissolved in EtOAc (5 mL) and washed with brine (5 mL). The organic layer was dried over anhyd Na₂ SO₄, filtered and concentrated. The crude product was purified on a preparative TLC (75% EtOAc in hexane) to give 30 mg (47 % yield) of the product as a colorless residue. mp 170° C. (dec); ¹ H NMR (CDCl₃) 7.12-7.38 (14H, m), 7.02 (1H, d, J=7.6 Hz), 5.28 (1H, dd, J=10.5, 6.4 Hz), 5.22 (1H, m), 4.32 (1H, m), 3.80 (2H, m), 3.52 (1H, m), 2.82-3.28 (10H, m), 2.42 (1H, m), 1.99 (2H, m), 1.27 (9H, s); MS (M+1)=586; HRMS (M+1)=586.3284 15, calcd for C₃₅ H₄₄ N₃ O₅ 586.328096.

Analysis C₃₅ H₄₃ N₃ O₅.0.6 CH₂ Cl₂ C:67.15; H:7.00; N:6.60 Found:(obsd) C:67.05; H:7.00; N:6.55

EXAMPLE 2 Step 1 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-1-phenyl-4-penten-3-one, compound 12

To a magnetically stirred solution of vinylmagnesium bromide in THF (0.5 M solution, 122 mL, 61.0 mmol) was added a solution of N',N'-methoxymethyl-N-tert-butyloxycarbonylphenylalanine carboxamide (4.70 g, 15.24 mmol) in 30 mL THF dropwise over a period of 30 min at -40°≠-25° C. The mixture was stirred for 4 h while the reaction temperature was allowed to warm up to 20° C. When there was no starting material by TLC, 10% citric acid solution (50 mL) was added to the mixture and it was extracted with ethyl ether (2×50 mL) and the ether extracts were combined. The combined organic solution was washed with sat aq NaHCO₃ solution (50 mL), water (50 mL), and brine (50 mL), and dried over anhyd MgSO₄. Filtered solution was concentrated to give a pale yellow residue, which was used for the next step without further purification. ¹ H NMR (CDCl₃) 7.10-7.36 (5H, m), 6.46 (1H, dd, J=9.8, 17.8 Hz), 6.37 (1H, dd, J=1.7, 17.5 Hz), 5.87 (1H, dd, J=l.7, 9.8 Hz), 5.25 (1H, d, J=6.8 Hz), 4.99 (1H, m), 3.17 (1H, ABX, J_(AB) =13.9 Hz, J_(AX) =6.4 Hz), 3.01 (1H, ABX, J_(AB) =13.2 Hz, J_(BX) =5.6 Hz), 1.44 (9H, s).

Step 2 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-ethenyl-3(R )-hydroxy-1-phenyl-5-hexene, compound 13

To a magnetically stirred suspension of CeCl₃ in THF (50 mL) was added a THF solution of allylmagnesium bromide (1.0 M, 10.25 mL) at 0° C. The mixture was stirred for 1.5 h at 0° C. and the solution turned to deep purple. Compound 12 (1.129 g, 4.10 mmol) in 5 mL THF was dropwise to the reaction mixture at 0° C. and the reaction mixture turned pale yellow. Stirring was continued for 1.5 h at 0° C. Citric acid solution (10% aq. 20 mL) was added to the reaction mixture and it was extracted with ether (2×20 mL). The organic layer was washed with sat aq NaHCO₃ solution (20 mL) and brine (20 mL). Drying (over anhyd MgSO₄) followed by concentration provided a crude product, which was purified on a silica gel chromatographic column to provide 1.86 g (56%) of compound 13. ¹ H NMR (CDCl₃) 7.15-7.32 (5H, m), 5.93 (1H, dd, J=10.7, 17.3 Hz), 5.83 (1H, m), 5.41 (1H, dd, J=1.5, 17.3 Hz), 5.33 (1H, d, J=10.8 Hz), 5.12-5.31 (2H, m), 4.71 (1H, d, J=9.8 Hz), 3.87 (1H, m), 3.06 (1H, ABX, JAB=14.2, J_(AX) =3.2 Hz), 2.59 (1H, ABX, J_(AB) =14.2, J_(BX) =11.1 Hz), 2.48 (2H, m), 1.32 (9H, s), 1.16 (1H, br s).

Step 3 Preparation of (4S)-phenylmethyl-3-N-(1,1-dimethylethoxy-carbonyl)-5(R)-ethenyl-5(R)-(2'-propenyl)oxazolidin-2-one compound 14

Compound 14 was prepared in the same manner as compound 5. ¹ H NMR (CDCl₃) 7.16-7.32 (5H, m), 5.52-5.70 (2H, m), 5.10-5.34 (4H, m), 4.38 (1H, dd, J=5.7, 7.6 Hz), 2.96 (1H, ABX, J_(AB) =15.0 Hz, J_(AX) =5.7 Hz), 2.82 (1H, A_(B) X, J_(AB) =15.0 Hz, J_(BX) =7.6 Hz), 2.38 (2H, m), 1.43 (9H, s).

Step 4 Preparation of N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(R)-hydroxy-3'(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane-amide, compound 16

Compound 16 was prepared from compound 14 in the same manner as compound 7 was prepared from compound 5. mp 82°-86° C. (dec); ¹ H NMR (CDCl₃) 7.12-7.34 (14H, m), 7.04 (1H, d, J=5.9 Hz), 6.63 (1H, d, 7.6 Hz), 5.26 (1H, dd, J=8.7, 5.1 Hz), 5.05 (1H, d, J=9.5 Hz), 4.33 (1H, m), 4.03 (1H, m), 3.41 (1H, m), 3.62 (1H, m), 2.84-3.31 (9H, m), 2.31 (1H, br s), 2.09 (1H, m), 1.86 (1H, m), 1.33 (9H, s);

Analysis calculated for C₃₅ H₄₃ N₃ O₅.0.5 CHCl₃ C:66.06; H:6.79; N:6.51 Found:(obsd) C:66.28; H:6.96; N:6.18

EXAMPLE 3 Step 1 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-1-phenyl-6-hepten-3-one, compound 17

To a magnetically stirred suspension of Mg (6.16 g, 0.254 mol) in ether (200 mL) was added 1-bromo-3-butene (26.31 g, 0.195 mol) dropwise over a period of 30 min. Stirring was continued for 0.5 h. 150 mL THF was added to the solution and the mixture was cooled to -40° C. N',N'-methoxymethyl-N-tert-butyloxycarbonylphenylalanine carboxamide (10.0 g, 32.5 mmol) in THF (10 mL) was added dropwise over a period of 25 min. Stirring was continued for 1.5 h while the flask was allowed to warm up to room temperature. When there was no starting material by TLC, 10% citric acid solution (100 mL) was added to the mixture and it was extracted with ethyl ether (3×50 mL.). Combined organic solution was washed with sat aq NaHCO₃ solution (200 mL), and brine (150 mL), and dried over anhyd Na₂ SO₄. Filtered solution was concentrated and the residue was washed with hexane to remove excess 1-bromo-3-butene. After removal of solvents under high vacuum, 6.40 g (65% yield) of compound 13 was obtained as a colorless crystal. ¹ H NMR (CDCl₃) 7.12-7.33 (5H, m), 5.73 (1H, m), 5.11 (1H, d, J=7.3 Hz), 4.97 (2H, m), 4.53 (1H, m), 3.05 (1H, ABX, J_(AB) =13.7 Hz, J_(AX) =6.6 Hz), 2.95 (1H, ABX, J_(AB) =13.7 Hz, J_(BX) =6.3 Hz), 2.47 (2H, m), 2.27 (2H, m), 1.41 (9H, s).

Step 2 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-ethenyl-3(S)-hydroxy-1-phenyl-6-heptene, compound 18

To a magnetically stirred solution of vinylmagnesium bromide in THF (1.0 M, 63.2 mL) at -40° C. was added a THF solution (20 mL) of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-1-phenyl-6-hepten-3-one (6.386 g, 21.1 mmol) over a period of 10 min. The mixture was stirred for 1 h while the temperature was allowed to warm up to 15° C. After addition of 10% aq citric acid solution (100 mL), the mixture was diluted with ether (100 mL) and layers separated. The aq layer was extracted with ether (2×50 mL) and the organic layers combined. The combined organic layers were washed with sat aq NaHCO₃ solution (2×200 mL) and brine (150 mL). Drying over anhyd Na₂ SO₄ followed by concentration provided a crude product, which was purified on a silica gel chromatographic column to provide 2.89 g (42% yield) of compound 18. ¹ H NMR (CDCl₃) 7.15-7.32 (5H, m), 5.81-5.96 (2H, m), 5.22-5.42 (2H, m), 4.95-5.12 (2H, m), 4.52 (1H, d, J=7.6 Hz), 3.72 (1H, m), 3.13 (1H, ABX, J_(AB) =13.0, J_(AX) =4.4 Hz), 2.82 (1H, br s), 2.66 (1H, ABX, J_(AB) =13.1, J_(BX) =11.4 Hz), 2.25 (2H, m), 1.82 (1H, m), 1.67 (1H, m), 1.25 (9H, s).

Step 3 Preparation of N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(3'(S)-hydroxy-3'-(1"(S)-tert-butyloxycarbonylamino-2"-phenyl)ethylpiperidinyl-3-cyclohexylpropaneamide, compound 19

To a magnetically stirred solution of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-ethenyl-3(S)-hydroxy-1-phenyl-6-heptene (0.196 g, 0.591 mmol) in 5 mL methanol at -78° C. was bubbled in ozone the mixture turned blue. Dimethyl sulfide (0.5 mL) was added at -78° C. and the mixture was warmed to room temperature. Solvent was removed under reduced pressure. The residue was dissolved in methanol (3 mL) and N-tert-butyl-2(S)-amino-3-cyclohexylpropanamide•hydrochloride (0.186 g, 0.710 mmol), NaCNBH₃ (0.223 g, 3.55 mmol) and acetic acid (0.081 mL, 1.42 mmol) were added. Stirring was continued for 24 h. The reaction mixture was then partitioned between sat aq Na₂ CO₃ solution (10 mL) and EtOAc (10 mL) and the aqueous layer was extracted with EtOAc (5 mL×2). Combined organic layers were dried over anhyd Na₂ SO₄, filtered and concentrated under reduced pressure. The crude product was purified on a silica gel column chromatography (75% EtOAc in hexane) to provide 61.3 mg (20% yield) of compound 19 as a colorless residue. UV (1 max)=259 nm; ¹ H NMR (CDCl₃) 7.12-7.32 (5H, m), 6.55 (1H, br s), 4.72 (1H, d, J=8.9 Hz), 3.88 (1H, m), 3.08 (1H, ABX, J_(AB) =13.9 Hz, J_(AX) =5.1 Hz), 2.82-3.0 (1H, m), 2.63 (1H, ABX, J_(AB) =14.0 Hz, J_(BX) =11.4 Hz), 2.44-2.7 (3H, m), 2.15-2.30 (1H, m), 1.1-1.85 (17H, m), 1.32 (9H, s), 1.15 (9H, s).

Analysis calculated for C₃₁ H₅₁ N₃ O₄.0.1 CHCl₃ C:68.95; H:9.51; N:7.76 Found:(obsd) C:68.78; H:9.45; N:8.07

EXAMPLE 4 Step 1 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylamino)-3-(2'-propenyl)-3-hydroxy-1-phenyl-5-hexene, compound 20

Compound 20 was prepared in the same way as compound 4.4. was prepared from compound 3. ¹ H NMR (CDCl₃) 7.18-7.32 (5H, m), 5.95 (2H, m), 5.16-5.27 (4H, m), 4.56 (1H, d, J=7.6 Hz), 3.99 (1H, m), 3.12 (1H, ABX, J_(AB) =14.5 Hz, J_(AX) =3.2 Hz), 2.67 (1H, ABX, J_(AB) =14.5 Hz, J_(BX) =11.4 Hz), 2.31-2.49 (4H, m), 1.28 (9H, s).

Step 2 Preparation of N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(4'(S)-hydroxy-4'(S)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)piperidinyl)-3-phenylpropane-amide, compound 21

Compound 21 was prepared in the same manner from compound 20 as compound 19 from compound LB., 35% yield. mp 193°-195° C.; UV (1 max)=264 nm; ¹ H NMR (CDCl₃) 7.15-7.32 (14H, m), 7.09 (1H, d J=6.0 Hz), 5.30 (1H, dd, J=4.9, 8.3 Hz), 4.69 (1H, d, J=8.9 Hz), 3.53 (1H, m), 3.40 (1H, m), 3.26 (1H, ABX, J_(AB) =13.6 Hz, J_(AX) =8.4 Hz), 2.96-3.24 (3H, m), 2.62-2.89 (7H, m), 2.45 (1 H, br s), 1.59-1.76 (4H, m), 1.31 (9H, s).

Analysis calculated for C₃₆ H₄₅ N₃ O₅.0.12 CHCl₃ C:70.64; H:7.41; N:6.84 Found:(obsd) C:70.68; H:7.50; N:6.75

EXAMPLE 5 Step 1 Preparation of (2S)-N-(1,1-dimethylethoxy-carbonylsamino)-5-methyl-1-phenyl-4-hexen-3-one, Compound 22

A THF solution of 2-methyl-1-propenylmagnesium bromide is prepared according to the procedure of D. A. Boyles and D. E. Nichols (J. Org. Chem. 1988, 53, 5128-5130). Using the THF solution of 2-methyl-1-propenylmagnesium bromide, compound 22 is prepared (77% yield) in the same manner as compound 12 from compound 2. ¹ H NNMR (CDCl₃) 7.10-7.32 (5H, m), 6.08 (1H, s), 5.28 (1H, d, J=6.6 Hz), 4.55 (1H, m), 3.14 (1H, ABX, J_(AB) =14.1 Hz, J_(AX) =6.5 Hz), 2.98 (1H, ABX, J_(AB) =14.6 Hz, J_(BX) =5.6 Hz), 2.16 (3H, s), 1.91 (3H, s), 1.43 (9H, s).

Step 2 Preparation of (2S)-N-(1',1'-dimethylethyloxycarbonyl)amino-3(R)-hydroxy-3(R)-(2'-methyl-1'-propenyl)-1-phenyl-6-heptene, Compound 23

Compound 23 is prepared from compound 22 in the smae manner as compound 18 is prepared from compound 17.

Step 3 Preparation of N-tert-butyl-3-cyclohexyl-2(S)-(3'(R)-hydroxy-3"(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)-1'-piperidinyl)propoanamide, Compound 24

Compound 24 is prepared from compound 23 in the same manner as compound 19 is prepared from compound 18. mp 83°-88.5° C.; ¹ H NMR (CDCl₃) 7.18-7.36 (5H, m), 6.68 (1H, br s), 4.65 (1H, d, J=8.8 hz), 3.78 (1H, m), 3.04 (1H, A_(BX), J_(AB) =14.0 Hz, J_(AX) =5.0 Hz), 3.02 (1H, m), 2.74 (2H, m), 2.72 (1H, A_(BX), J_(AB) =14.0 Hz, J_(BX) =11.0 Hz), 2.41 (2H, m), 1.20-1.85 (17H, m), 1.41 (9H, s), 1.32 (9H, s).

Analysis calculated for C₃₁ H₅₁ N₃ O₄.0.2 CHCl₃ C:67.68; H:9.32; N:7.59 Found:(obsd) C:67.65; H:9.32; N:7.54

While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations, or modifications, as come within the scope of the following claims and its equivalents. 

What is claimed is:
 1. A compound of the Formula I ##STR171## m=0,1; n=0,1;R₁ and R₂ are independentlya) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; b) C₅ -C₇ cycloalkyl; or c) heterocycle unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; R₃ isa) hydrogen; b) C₁₋₆ alkyl, unsubstituted or substituted with one or more of hydroxy, C₁₋₃ alkoxy, aryl, heterocycle or halo; c) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; d) heterocycle unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; or e) a 5 to 7 membered carbocyclic or 7-10 membered bicyclic carbocyclic ring, the carbocyclic ring being unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; and T is R₄ OC(O), R₄ C(O) or R₄ NR₅ C(O) wherein R₄ isa) C₁₋₅ alkyl unsubstituted or substituted with one or more of aryl, heterocycle, hydroxy, halo or C₁₋₃ alkoxy; b) a 5- to 7-membered carbocycle or carbocycle-C₁₋₄ alkyl wherein the carbocycle is either saturated, partially saturated or unsaturated, any of which carbocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, C₁₋₃ alkoxy, halo-C₁₋₃ alkyl, aryl-C₁₋₃ alkyl, or C₃₋₅ cycloalkyl; c) a 5- to 7-membered heterocycle or heterocycle-C₁₋₄ alkyl wherein the heterocycle has one or two heteroatoms selected from O, N or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo, C₃₋₅ cycloalkyl, or C₁₋₃ alkoxy; d) aryl unsubstituted or substituted with one or more of C₁₋₄ lower alkyl, hydroxy, C₁₋₃ alkoxy or halo; or e) heterocycle; and R₅ isa) hydrogen, or b) C₁₋₄ alkyl unsubstituted or substituted with one or more of C₂₋₄ alkenyl, C₁₋₃ alkoxy, halo-C₁₋₃ alkyl, hydroxy-C₂₋₄ alkyl, aryl-C₁₋₃ alkyl, or C₃₋₅ cycloalkyl; and A is absent ora) an L-amino acid residue chosen from valine, isoleucine, leucine, alanine, asparagine or serine; or b) 5- to 7-membered heterocycle or heterocycle-C₁₋₄ alkyl wherein the heterocycle has one or two heteroatoms selected from O, N or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo, C₃₋₅ cycloalkyl, or C₁₋₃ alkoxy, or pharmaceutically acceptable salt thereof.
 2. A compound according to claim 1 whereinA is absent; T is R₄ OC(O); R₁ and R₂ are independently phenyl or cyclohexyl, any of which is unsubstituted or substituted with hydroxy or C₁₋₃ alkoxy; R₃ is a C₁₋₅ alkyl, unsubstituted or substituted with one or more hydroxy or R₃ is 1(S)-(2(R)-hydroxyindan); and R₄ is a C₁₋₅ alkyl or a 5- to 7-membered heterocycle having one heteroatom selected from O or S, any of which heterocycle is unsubstituted or substituted with one or more of C₁₋₄ alkyl, C₂₋₄ alkenyl, oxo or C₁₋₃ alkoxy.
 3. A compound according to claim 2 whereinT is R₄ OC(O); R₁ and R₂ are phenyl; R₃ is t-butyl, 2-methylpropyl or 1(S)-(2(R)-hydroxyindan); and R₄ isi) C₁₋₅ alkyl; or ii) 1,1-dioxo-tetrahydrothienyl or tetrahydrofuranyl, unsubstituted or substituted with C₁₋₄ alkyl, C₂₋₄ alkenyl or C₁₋₃ alkoxy.
 4. A compound according to claim 3 whereinR₄ isi) C₁₋₅ alkyl; or ii) tetrahydrofuran-3-yl or 1,1-dioxotetrahydrothien-3-yl, unsubstituted or substituted with methyl, ethyl, n-propyl, i-propyl, methoxy, ethoxy, or propenyl.
 5. A compound according to claim 1 whereinR₁ and R₂ are phenyl; R₃ is 1(S)-(2(R)-hydroxyindan); and R₄ isi) C₁₋₅ alkyl; or ii) a 5- to 7-membered heterocycle having one S heteratom, said heterocycle unsubstituted or substituted with one or more of C₁₋₄ alkyl, oxo or C₃₋₅ cycloalkyl.
 6. A compound according to claim 5 whereinR₁ and R₂ are phenyl; R₃ is 1(S)-(2(R)-hydroxyindan); and R₄ isi) C₁₋₅ alkyl; or ii) 1,1-dioxotetrahydrothien-3-yl, unsubstituted or substituted with C₁₋₄ alkyl, or C₃₋₅ cycloalkyl.
 7. The compound: ##STR172## named: N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(S)-hydroxy-3'(S)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane amide;or pharmaceutically acceptable salt thereof.
 8. The compound: ##STR173## named: N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(1'-(3'(R)-hydroxy-3'(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)pyrrolidinyl))-3-phenylpropane-amide;or pharmaceutically acceptable salt thereof.
 9. The compound: ##STR174## named: N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(4'(S)-hydroxy-4'(S)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)piperidinyl)-3-phenylpropane-amide;or pharmaceutically acceptable salt thereof.
 10. The compound: ##STR175## named: N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(4'-hydroxy-4'(1"(S)-(3"'(S)-tetrahydrofuryloxycarbonyl)amino-2"-phenyl)ethyl-1'-piperidinyl)-3-phenylpropane-amide;or pharmaceutically acceptable salt thereof.
 11. The compound: ##STR176## named: N-(1'(S)-(2'(R)-hydroxyindanyl))-2(S)-(3'(S)-hydroxy-3'(S)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)-1'-piperidinyl)-3-phenylpropane-amide;or pharmaceutically acceptable salt thereof.
 12. The compound: ##STR177## named: N-(1',1'-dimethylethyl)-2(S)-(3'(R)-hydroxy-3'(R)-(1"(S)-tert-butyloxycarbonylamino-2"-phenylethyl)-1'-piperidinyl)-3-cyclohexylpropane-amideor pharmaceutically acceptable salt thereof.
 13. A pharmaceutical composition, for use in the treatment of AIDS, in the treatment of infection by HIV, or in the inhibition of HIV protease, comprising an effective amount of a compound as in any of claims 1-12, and a pharmaceutically acceptable carrier.
 14. A method of treating AIDS, comprising administering an effective amount of a con, poured as in any of claims 1-12.
 15. A method of treating infection by HIV, comprising administering an effective amount of a compound as in any of claims 1-12.
 16. A method of inhibiting HIV protease, comprising administering an effective amount of a compound as in any of claims 1-12. 